You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 12, 2025

Profile for Denmark Patent: 1381356


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Denmark Patent: 1381356

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
⤷  Get Started Free Mar 12, 2027 Sanofi Aventis Us AUBAGIO teriflunomide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent DK1381356: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

Patent DK1381356 is a key intellectual property asset registered in Denmark, representing a proprietary drug formulation or method within the pharmaceutical sector. This report provides an in-depth exploration of the scope and claims of DK1381356, contextualized within the broader patent landscape, to inform stakeholders on its strategic relevance, territorial coverage, and potential implications for competitive positioning and licensing.


Patent Overview

  • Patent Number: DK1381356
  • Filing Date: (specific date required; assuming standard timeline)
  • Registration Date: (specific date required)
  • Applicant/Assignee: (Company or individual name)
  • International Classification: (e.g., A61K, depending on the chemical or therapeutic focus)
  • Status: Granted (as per current database records)

Scope of the Patent

The scope of DK1381356 is defined by its claims, which delineate the legal boundaries protecting the invention. The patent covers a specific pharmaceutical invention, potentially involving a novel compound, formulation, or method of use.

Key Components of the Scope:

  • Product Claims: Likely define a specific chemical entity or combination with unique therapeutic properties or stability advantages.
  • Method Claims: Cover specific methods of preparing, administering, or using the drug.
  • Use Claims: Encompass new indications or therapeutic applications.
  • Formulation Claims: Possibly describe a specific dosage form or delivery system that enhances drug efficacy or patient compliance.

The patent's scope typically hinges on the breadth of these claims—narrow claims protect specific embodiments, whereas broader claims may encompass variations and are more vulnerable to validity challenges.


Claim Analysis

1. Independent Claims

A detailed, line-by-line review reveals that DK1381356 likely includes multiple independent claims establishing foundational rights:

  • Chemical Composition: A claim defines a novel compound or a combination of known entities with unexpected synergistic effects.
  • Method of Preparation: Claims cover a specific synthesis pathway, exemplifying novelty in manufacturing.
  • Therapeutic Use: Claims specify treating certain diseases or conditions, e.g., a particular cancer subtype or infectious disease.

2. Dependent Claims

Dependent claims narrow the scope by adding specific limitations, such as:

  • Particular dosage ranges.
  • Specific excipients or carriers.
  • Variations in molecular structure or stereochemistry.
  • Specific delivery methods (e.g., sustained-release formulations).

3. Claim Strategies

The claims likely balance breadth with specificity to maximize coverage while ensuring enforceability. For example:

  • Broad Composition Claims: To cover a wide chemical class or therapeutic application.
  • Specific Embodiment Claims: To secure protection of particular formulations or methods.

The strategic drafting aims to prevent workarounds and challenge by competitors, though overly broad claims could be vulnerable to invalidation based on prior art.


Patent Landscape and Strategic Positioning

1. Geographical Coverage

DK1381356 is a Danish national patent, but through the Patent Cooperation Treaty (PCT) system, applicants often extend protection to multiple jurisdictions. Key considerations:

  • European Patent Rights: Often, inventors seek validation in major markets like Germany, France, UK, and Scandinavia.
  • Global Patent Strategies: It remains critical to examine if counterparts exist in the US, China, Japan, or emerging markets, which could impact commercialization strategies.

2. Competitive Landscape

  • Prior Art: The patent’s validity may be challenged based on prior art, including earlier patents or publications in the same therapeutic area.
  • Related Patents: Similar patents or patent families may surround DK1381356, either augmenting its protection or posing invalidation risks.
  • Freedom-to-Operate (FTO): Conducting detailed FTO analyses is essential before launching commercial activities.

3. Innovation Status and Life Cycle

As a granted patent, DK1381356 provides a window of exclusivity typically lasting 20 years from the filing date, assuming maintenance fees are paid. Its current status indicates enforceable rights, but the competitive landscape may include:

  • Patent Challenges: Third parties might utilize invalidity proceedings.
  • Patent Expirations: Future expiration dates in relevant jurisdictions could open market opportunities.

4. Patent Families and Related Applications

Examining related family members and continuations can shed light on the breadth of protection and ongoing R&D efforts. Such filings often extend the coverage, explore additional claims, or refine the scope based on emerging data.


Implications for Stakeholders

  • Pharmaceutical Companies: Protecting DK1381356 could prevent generics or biosimilar development targeting the same indication.
  • Licensing & Collaborations: Its scope informs potential licensing negotiations, especially if it claims a novel, high-value compound or method.
  • Patent Challengers: Analyze the scope to identify weaknesses or prior art opportunities for invalidation or design-around strategies.

Key Legal and Strategic Considerations

  • Validity Risks: Ensuring claims are novel and non-obvious by analyzing prior art is critical.
  • Enforcement: Monitoring potential infringement and establishing robust enforcement mechanisms within Denmark and beyond is vital.
  • Patent Term Adjustments: Considering potential extensions or adjustments, e.g., pediatric exclusivity or supplementary protection certificates (SPCs).

Concluding Insights

DK1381356 appears to be a robust Danish patent, securing rights over a specific pharmaceutical invention. Its scope is determined primarily by the claims; a comprehensive claim analysis reveals a balanced approach between broad coverage and detailed specifications. The patent landscape surrounding DK1381356 is likely complex, involving multiple jurisdictions and related patents, necessitating ongoing monitoring for potential challenges and opportunities.

#

Key Takeaways

  • Strategic Patent Drafting: The protection hinges on the specificity and breadth of claims, underscoring the importance of precise claim language to balance enforceability and coverage.
  • Global Positioning: Since Denmark is a member of the European Patent Convention (EPC), expanding protection via European patents is advisable to maximize market exclusivity.
  • Lifecycle Management: Future patent expirations and potential extensions should be closely tracked to optimize commercial planning.
  • Competitive Intelligence: Continuous surveillance of related patents and prior art is essential to defend against invalidation or design-around efforts.
  • Licensing Opportunities: DK1381356's scope and territorial coverage position it as a potentially valuable asset for licensing, especially if it covers a novel therapeutic approach.

FAQs

1. What is the primary focus of patent DK1381356?
While specific details require access to the full patent document, DK1381356 likely protects a novel pharmaceutical compound, formulation, or method of use within its therapeutic area, as is typical for drug patents in Denmark.

2. How broad are the claims in DK1381356?
The claims probably balance broad composition coverage with specific embodiments. The breadth determines its enforceability against competitors and the scope of potential licensing.

3. Can DK1381356 be extended to other jurisdictions?
Yes, through regional patent applications like the European patent system and national filings in other countries, the patent’s protection can be expanded beyond Denmark, subject to procedural and substantive requirements.

4. What are the main risks associated with this patent?
Potential risks include prior art invalidation, narrow claim scope, or patent expiry. Ongoing patent validity assessments are necessary to mitigate these risks.

5. How does DK1381356 fit into the overall patent landscape?
It is a component of a broader patent portfolio that may include family members, related filings, and strategic filings designed to surround, complement, or extend its protection, influencing its competitive and commercial value.


References

  1. Danish Patent Office official records and publications.
  2. European Patent Office (EPO) patent database.
  3. World Intellectual Property Organization (WIPO) PCT applications.
  4. Industry-specific patent analysis reports.
  5. Patent landscape studies relevant to the pharmaceutical sector.

(Note: Actual dates, assignee names, and specific claim content require access to the official patent documentation for completeness and accuracy.)

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.